Canonical Allele Identifier: CA10637126

Gene: RDX

Linked Data

• ClinVar Variation Id: 302359
• ClinVar RCV Id: RCV000276183
• dbSNP Id: rs575111883
• gnomAD v2: 11-110167276-G-A
• gnomAD v3: 11-110296551-G-A
• gnomAD v4: 11-110296551-G-A
• MyVariant Identifiers: chr11:g.110167276G>A (hg19) ; chr11:g.110296551G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.110296551G>A , CM000673.2:g.110296551G>A	GRCh38
NC_000011.9:g.110167276G>A , CM000673.1:g.110167276G>A	GRCh37
NC_000011.8:g.109672486G>A	NCBI36
NG_023044.1:g.5162C>T
NG_023044.2:g.5162C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000645495.2:c.-149C>T MANE Select	ENSP00000496503.2:n.-149C>T
ENST00000645527.1:c.-357C>T	ENSP00000496121.1:n.-357C>T
ENST00000647231.1:c.-149C>T	ENSP00000496414.1:n.-149C>T
ENST00000343115.8:c.-149C>T	ENSP00000342830.4:n.-149C>T
ENST00000405097.5:c.-149C>T	ENSP00000384136.1:n.-149C>T
ENST00000528498.5:c.-149C>T	ENSP00000432112.1:n.-149C>T
ENST00000528556.5:c.-149C>T	ENSP00000434881.1:n.-149C>T
ENST00000528900.5:c.-243C>T	ENSP00000433580.1:n.-243C>T
ENST00000530131.5:c.-149C>T	ENSP00000432829.1:n.-149C>T
ENST00000530301.5:c.-149C>T	ENSP00000436277.1:n.-149C>T
ENST00000530749.5:c.-149C>T	ENSP00000437301.1:n.-149C>T
ENST00000533678.1:c.-149C>T	ENSP00000435930.1:n.-149C>T
ENST00000533991.1:c.-106C>T	ENSP00000432572.1:n.-106C>T
ENST00000534683.1:c.-266C>T	ENSP00000431560.1:n.-266C>T
ENST00000544551.5:c.-186C>T	ENSP00000445826.1:n.-186C>T
NM_001260492.1:c.-149C>T	NP_001247421.1:n.-149C>T
NM_001260493.1:c.-149C>T	NP_001247422.1:n.-149C>T
NM_001260494.1:c.-186C>T	NP_001247423.1:n.-186C>T
NM_001260495.1:c.-243C>T	NP_001247424.1:n.-243C>T
NM_001260496.1:c.-149C>T	NP_001247425.1:n.-149C>T
NM_002906.3:c.-149C>T	NP_002897.1:n.-149C>T
NM_001260492.2:c.-149C>T	NP_001247421.1:n.-149C>T
NM_002906.4:c.-149C>T MANE Select	NP_002897.1:n.-149C>T
NM_001260493.2:c.-149C>T	NP_001247422.1:n.-149C>T
NM_001260494.2:c.-186C>T	NP_001247423.1:n.-186C>T
NM_001260495.2:c.-243C>T	NP_001247424.1:n.-243C>T
NM_001260496.2:c.-149C>T	NP_001247425.1:n.-149C>T